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Cat. No. Product Name Information
PC-28301

EDG-7500

Cardiac sarcomere modulator, Myofibril ATPase inhibitor

EDG-7500 is a diastolic-selective cardiac sarcomere modulator (d-CSM) that preferentially inhibits cardiac myofibril ATPase activity with EC25 value of 3.0 nM at diastolic calcium levels, with limited activity at systolic calcium levels (EC25>100 uM).
PC-24900

MT-110

Non-muscle myosin II inhibitor

MT-110 is a potent, selective, brain penetrant non-muscle myosin II (NMII) inhibitor with EC50 of 0.68 uM in cytokinesis assays, >70-fold selectivity over cardiac muscle myosin II (CMII).
PC-24862

MT-125

non-muscle myosin II inhibitor

MT-125 is a specific, brain penetrant small-molecule inhibitor of non-muscle myosin IIA and IIB (NMIIA and IIB) with Ki of 2.7 uM (NMIIA) and EC50 of 1.7 uM (NMIIB).
PC-24122

Delocamten

Cardiac myosin inhibitor

Delocamten (MYK-224, BMS-986435) is a potent selective cardiac myosin inhibitor with potential treatment of hypertrophic cardiomyopathy (HCM).
PC-23405

Adhibin

class-IX myosins inhibitor

Adhibin is a selective and allosteric inhibitor of RhoGAP class-IX myosins that abrogates ATPase and motor function, suppressing RhoGTPase-mediated modes of cancer cell metastasis.
PC-23211

MT-228

non-muscle myosin II inhibitor

MT-228 is a potent, selective, first-in-class non-muscle myosin II (NMII) inhibitor with Ki of 1.5 uM and cytokinesis EC50 of 1.0 uM, 17-fold selectivity for NMII over cardiac myosin II (CMII).
PC-23161

ML-7 hydrochloride

MLCK inhibitor

ML-7 hydrochloride is a potent, specific myosin light chain kinase (MLCK) inhibitor with IC50 of 300 nM, also inhibits YAP/TAZ.
PC-22762

Ulacamten

Cardiac myosin inhibitor

Ulacamten (CK-4021586, CK-586) is a potent, selective and oral cardiac myosin inhibitor, inhibits the ATPase activity of two-headed heavy meromyosin (HMM) but not single-headed subfragment-1.
PC-22347

Blebbistatin

Non-muscle myosin II inhibitor

Blebbistatin is a selective non-muscle myosin II (NMII) inhibitor, promotes directional migration of corneal endothelial cells (CECs) and accelerates wound healing, and better preserves cell junctional integrity and barrier function.
PC-22342

Divertin

MLCK1 inhibitor

Divertin (NSC55937, Tetraformaltrisazine) is a small molecule MLCK1 inhibitor, diverts MLCK1 from the PAMR, does not interfere with MLCK enzymatic activity, prevent MLCK-mediated intestinal barrier loss in vitro and in vivo.
PC-20390

Sevasemten

Myosin inhibitor

Sevasemten (EDG-5506) is a potent, selective, orally active inhibitor of fast skeletal muscle myosin, inhibits fast myofibril ATPase from rabbit psoas muscle with IC50 of 0.2 uM.
PC-72702

MT-134

SkMII inhibitor

MT-134 (Skeletostatin MT-134) is a selective skeletal myosin II (SkMII) inhibitor with Ki of 0.48 uM, 40- to 170-fold for SkMII over all other myosin II family members.

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